Effect of chromium aging on the structural and thermal properties of chromium polyacrylate

The effects of aging time of Cr(III) solutions on the structural, thermal, magnetic, and morphological properties of chromium polyacrylate complexes were studied. Chromium retention was found to increase with longer aging periods. IR spectra revealed the formation of polychelate structures with noticeable changes on aging. The interaction of multivalent, polynuclear Cr(III) species with the polymer backbone resulted in a decrease in thermal stability for the complexes prepared from olated chromium solutions. © 2005 Wiley Periodicals, Inc. J Appl Polym Sci 98: 490–493, 2005     

液体消毒洗涤剂的研制

研制了具有消毒杀菌、洗涤去污双重功效的液体消毒洗涤剂 ,测定了其对金黄色葡萄球菌的杀灭效果。结果表明 ,消毒洗涤剂的杀菌效果随其浓度的增加 ,作用时间的延长而提高 ;戊二醛浓度为 2 0 0× 10 -6时 ,与金黄色葡萄球菌作用 5min ,杀灭率可达 99.99%。将消毒洗涤剂在室温下放置半年 ,戊二醛分解率为 17.3 1%     

Activities of MFI-Supported Rhenium Catalysts for the Aromatization of Methane: Effect of Cationic Form of the Inorganic Carrier

MFI type inorganic carrier was used in two different cationic forms, hydrogen and calcium respectively. MFI-supported molybdenum and rhenium catalysts were prepared. The activities of the catalysts were compared for the aromatization reaction of methane. Higher activity values were attained with the catalysts supported on HZSM-5. Aromatics were also observed with the catalysts supported on CaZSM-5, despite their deficiency in acid sites. Highly dispersed rhenium is expected to be formed with the use of the inorganic carrier in calcium form. On the other hand, lower reaction rates were observed with rhenium supported on CaZSM-5, in spite of the improved dispersion of the active rhenium species on this catalyst. This was interpreted in terms of the critical role of the acid sites in the conversion of methane to aromatics, compared to the improved dispersion of the active metal.     

药用中间体苯丙酮含量的气相色谱/质谱分析

苯丙酮是合成利胆药苯丙醇的重要中间体。本文建立了用气相色谱 /质谱法 (GC/MS)测定苯丙酮含量的方法。组分的定性依靠GC/MS联用技术和NIST谱库标准质谱图对照分析。以苯乙酮为内标 ,苯丙酮含量在 1.0× 10 -5～ 2 .0× 10 -4g/mL范围内呈线性 ,线性相关系数r =0 .994 9,苯丙酮最低检测浓度为 1.0× 10 -8g/mL。该法操作简便、快速 ,结果准确可靠 ,且具有很好的实用价值     

Łukasiewicz logic and Riesz spaces

We initiate a deep study of Riesz MV-algebras which are MV-algebras endowed with a scalar multiplication with scalars from \([0,1]\) . Extending Mundici’s equivalence between MV-algebras and \(\ell \) -groups, we prove that Riesz MV-algebras are categorically equivalent to unit intervals in Riesz spaces with strong unit. Moreover, the subclass of norm-complete Riesz MV-algebras is equivalent to the class of commutative unital C \(^*\) -algebras. The propositional calculus \({\mathbb R}{\mathcal L}\) that has Riesz MV-algebras as models is a conservative extension of ?ukasiewicz \(\infty \) -valued propositional calculus and is complete with respect to evaluations in the standard model \([0,1]\) . We prove a normal form theorem for this logic, extending McNaughton theorem for ? ukasiewicz logic. We define the notions of quasi-linear combination and quasi-linear span for formulas in \({\mathbb R}{\mathcal L},\) and relate them with the analogue of de Finetti’s coherence criterion for \({\mathbb R}{\mathcal L}\) .     

Sol–Gel Processing and Microwave Characteristics of Ba(Mg⅓Ta⅔)O3 Dielectrics

The sol–gel method has been developed for the preparation of pure Ba(Mg_1/3Ta_2/3)O₃ ceramics. This involves the reaction of the heterometallic alkoxide Ta₂Mg(OEt)₁₂ with hydrated barium hydroxide Ba(OH)₂·8H₂O. Complete crystallization of the sol–gel-derived powder is achieved at 600°C, leading to a cubic perovskite type phase. After sintering at 1400°C (2–5 h), a trigonal cell arises from Mg–Ta ordering (the degree of order is greater than 0.9), and about 98.5% of the theoretical density is obtained. Preliminary microwave dielectric measurements show that the dielectric constant and the unloaded Q _u of the ceramics are 24.2 and 6750, respectively, at 7.7 GHz.     

Blends,hydrogen bonds,and orientation: Understanding the role of interactions

A review of past and present studies on orientation, rheology, and FTIR investigations on a hydrogen bond–forming polymer, poly(vinyl phenol) (PVPh), and its blends with polyethylene oxide (PEO), poly(methyl methacrylate) (PMMA), and poly(vinyl methyl ether) (PVME) is presented. Orientation is analyzed on the basis of deformation‐induced orientation and relaxation. For deformation, it is proposed from recent molecular modeling studies that orientation is similar for flexible backbone polymers of the types studied. To investigate relaxation, dynamical rheology analysis was performed previously on PVPh/PEO blends and global molecular weight between entanglement, M_e, and chain friction ζ were estimated. M_e remained close to that of the polymer forming the dominant network, a discontinuity being observed near 50 mole percent. Friction coefficient exhibited a maximum near that of the orientation function of this system. Near‐infrared measurements also showed a maximum in the number of interchain hydrogen bonds at this concentration, although broader than that of orientation or of the friction coefficient. For strongly interacting blends, it is proposed that a break in orientation behavior would be associated with the dominant network present, and therefore to M_e, whereas ζ will dictate whether orientation decreases or increases in a given network domain.     

Influence of the preparation conditions on the properties of gold catalysts for the oxidation of glucose

In this work, two deposition–precipitation methods for the preparation of gold catalysts for glucose oxidation were investigated. Thus far, gold colloids immobilized on carbon have been used for catalytic glucose oxidation, but the long-term stability of these systems was not sufficient. To improve the long-term stability we used the deposition–precipitation methods using NaOH (DP NaOH) or urea (DP urea) as precipitation agents as they were described by Haruta and Dekkers, respectively, using alumina as a support material. With these methods, it was possible to prepare highly active and selective catalysts which showed an excellent long-term stability. DP urea was found to be the preferred method, because in contrast to DP NaOH, no losses of gold occurred during the preparation, and it was possible to adjust various gold contents up to 10 wt% Au.